Nguyen V C, Aubert J P, Gross M S, Porchet N, Degand P, Frézal J
Laboratorie de Cytogénétique et de Génétique Oncologiques URA 1158 CNRS, Institut Gustave Roussy, Villejuif, France.
Hum Genet. 1990 Dec;86(2):167-72. doi: 10.1007/BF00197699.
Extensive heterogeneity of tracheobronchial mucin RNAs has been described recently. Based on the results of total or partial cDNA sequencing, the mucin cDNAs obtained were classified into three groups. The first group contained 24 bp tandem repeat sequences, the second exhibited homology at their amino- and carboxyl-terminals, and the third group seems to consist of alternative hydrophilic-hydrophobic zones. JER58, JER47 and JER57 probes, representing the first, second, and third tracheobronchial mucin families respectively, were used for chromosome assignment. In human DNAs digested with BamHI, the JER58 probe detected a sequence of 21 kb, the JER47 probe detected a major sequence of 21 kb and a minor sequence of 4 kb, and the JER57 probe detected two sequences of 1.8 kb and 1.3 kb. By somatic hybrid cell analysis, the JER58. JER47, and JER57 major sequences were assigned to chromosome 11 and the JER47 minor sequence to chromosome 13. By in situ hybridization the JER58, JER47 and JER57 probes were assigned to 11p15. Under the experimental conditions used, no specific hybridization to the chromosome 13 region was observed with the JER47 probe. Our results indicate that tracheobronchial mucin gene(s) is/are localized on 11p15. The minor JER47 BamHI sequence localized on chromosome 13 probably corresponds to a tracheal-mucin related sequence. The intestinal mucin gene was also recently localized to the same 11p15 region. Intestinal and tracheobronchial mucins appear different according to their tissue distribution and their cDNA nucleotide sequences. Tracheal mucin probes (JER58, JER47, JER57) and intestinal probes may represent independent genes on 11p15 or else different mRNAs from the same primary transcript produced by differential splicing. Further studies using mucin genomic probes for 11p15 will be required for the elucidation of tracheal and intestinal mucin gene organisation in this region.
最近已报道气管支气管粘蛋白RNA存在广泛的异质性。根据全长或部分cDNA测序结果,所获得的粘蛋白cDNA被分为三组。第一组含有24bp串联重复序列,第二组在其氨基末端和羧基末端表现出同源性,第三组似乎由交替的亲水-疏水区域组成。分别代表第一、第二和第三气管支气管粘蛋白家族的JER58、JER47和JER57探针被用于染色体定位。在用BamHI消化的人DNA中,JER58探针检测到一个21kb的序列,JER47探针检测到一个21kb的主要序列和一个4kb的次要序列,JER57探针检测到两个1.8kb和1.3kb的序列。通过体细胞杂交细胞分析,JER58、JER47和JER57的主要序列被定位于11号染色体,JER47的次要序列定位于13号染色体。通过原位杂交,JER58、JER47和JER57探针被定位于11p15。在所用的实验条件下,未观察到JER47探针对13号染色体区域的特异性杂交。我们的结果表明气管支气管粘蛋白基因定位于11p15。定位于13号染色体的JER47 BamHI次要序列可能对应于一个气管粘蛋白相关序列。肠粘蛋白基因最近也被定位于相同的11p15区域。肠粘蛋白和气管支气管粘蛋白根据其组织分布和cDNA核苷酸序列而有所不同。气管粘蛋白探针(JER58、JER47、JER57)和肠探针可能代表11p15上的独立基因,或者是由差异剪接产生的来自同一初级转录本的不同mRNA。为了阐明该区域气管和肠粘蛋白基因的组织情况,需要使用针对11p15的粘蛋白基因组探针进行进一步研究。